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Volumn 32, Issue 6, 2005, Pages 500-502

The common KRT9 gene mutation in a Japanese patient with epidermolytic palmoplantar keratoderma and knuckle pad-like keratoses [1]

Author keywords

Direct sequencing; Genotype phenotype correlation; Mechanical friction; PCR

Indexed keywords

KERATIN; KERATIN 9; UNCLASSIFIED DRUG;

EID: 22344456352     PISSN: 03852407     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1346-8138.2005.tb00789.x     Document Type: Letter
Times cited : (9)

References (10)
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  • 2
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  • 3
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  • 4
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    • Epidermolytic palmoplantar keratoderma of Vorner: Re-evaluation of Vorner's original family and identification of a novel keratin 9 mutation
    • Kuster W, Reis A, Hennies HC: Epidermolytic palmoplantar keratoderma of Vorner: re-evaluation of Vorner's original family and identification of a novel keratin 9 mutation, Arch Dermatol Res, 294: 268-272, 2002.
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  • 5
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  • 6
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    • Mutations of keratin 9 in two families with palmoplantar epidermolytic hyperkeratosis
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  • 7
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  • 8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.